Variant (rsID / SNP)
rs5030655
rs5030655 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2D6. Location: chromosome 22, position 42,525,086. Clinical significance in the table: Likely benign; drug response; other.
Reference-table entries
CYP2D6Likely benign
- Clinical significance (as recorded)
- Likely benign; drug response; other
- Variant type
- Deletion
- Chromosome / position
- 22:42525086
- Cytoband
- 22q13.2
- HGVS
- CYP2D6*6
Associated conditions / phenotypes
Debrisoquine, poor metabolism of|Deutetrabenazine response|Tamoxifen response
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.